51351-79-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(2,2-Dimethylpropyl)benzoic acid is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, 2-(2,2-Dimethylpropyl)benzoic acid is used as a chemical intermediate to produce a range of dyes that are utilized in coloring textiles, plastics, and other materials.
Used in Agrochemical Industry:
2-(2,2-Dimethylpropyl)benzoic acid is employed as a precursor in the production of agrochemicals, contributing to the development of pesticides and other agricultural chemicals that enhance crop protection and yield.
Used in Plastics Industry:
In the plastics industry, 2-(2,2-Dimethylpropyl)benzoic acid is used in the manufacturing of high-performance thermoplastics, where it imparts desirable properties such as strength, durability, and heat resistance to the final products.
Used in Industrial Chemicals and Additives Production:
2-(2,2-Dimethylpropyl)benzoic acid is utilized in the production of various industrial chemicals and additives, where it serves as a key component in the formulation of products used across different sectors, including coatings, adhesives, and lubricants.
Check Digit Verification of cas no
The CAS Registry Mumber 51351-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,5 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51351-79:
(7*5)+(6*1)+(5*3)+(4*5)+(3*1)+(2*7)+(1*9)=102
102 % 10 = 2
So 51351-79-2 is a valid CAS Registry Number.
51351-79-2Relevant academic research and scientific papers
Intramolecular Reactivity of Arylcarbenes: Derivatives of o-Tolylcarbene
Kirmse, Wolfgang,Konrad, Wolfgang,Schnitzler, Dirk
, p. 3821 - 3829 (2007/10/02)
Various CH2X groups have been attached to the ortho position of phenylcarbene.If 2'- or 3'-C-H bonds are present, as in 23 (X = Me), 71 (X = CMe3), and 58 (X = SiMe3), C-H insertion leading to five- or six-membered rings predominates in the gas phase and competes with intermolecular reactions in solution.The formation of benzocyclobutenes via insertion into 1'-C-H bonds is a very minor reaction path of 23 and 71.In contrast, 58 produces substantial amounts of the benzocyclobutene 59 by way of C-Si insertion, particularly in the gas phase.Insertion into the Si-Me bonds of 58 also occurs while the C-F bonds of 37 (X = CF3) and 50 (X = F) are inert.In the gas phase, 37 and 50 give mainly benzocyclobutenes whereas intermolecular reactions prevail in solution.The effects of sensitization and of solvent polarity suggest that benzocyclobutenes arise from singlet arylcarbenes.The amount of carbene-carbene rearrangement decreases in the order 7 (X = H) > 37 (X = CF3) > 23 (X = Me); no rearrangement was observed with 50 (X = F), 58 (X = SiMe3), and 71 (X = CMe3).
